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用于基于智能手机比色检测蛋白酶生物标志物的蛋白水解响应转录与球形核酸的模块化组合

Modular Combination of Proteolysis-Responsive Transcription and Spherical Nucleic Acids for Smartphone-Based Colorimetric Detection of Protease Biomarkers.

作者信息

Liu Fang, Chen Ru, Song Wenlu, Li Liangwen, Lei Chunyang, Nie Zhou

机构信息

State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan Provincial Key Laboratory of Biomacromolecular Chemical Biology, Hunan University, Changsha 410082, P. R. China.

出版信息

Anal Chem. 2021 Feb 23;93(7):3517-3525. doi: 10.1021/acs.analchem.0c04894. Epub 2021 Feb 5.

Abstract

Sensitive and facile detection of biomarkers is essential for early diagnosis and treatment of diseases. To this end, we here proposed a colorimetric protease assay by the modular combination of proteolysis-responsive transcription and spherical nucleic acids (SNAs). In this assay, target protease-mediated proteolysis triggers the synthesis of RNAs by transcription, which subsequently results in the aggregation of SNAs with remarkable redshifts in the wavelength of surface plasmon resonance-related absorption. As a proof of concept, this assay achieved the sensitive and specific detection of matrix metalloprotease-2 (MMP-2) with a limit of detection of 3.3 pM. Moreover, the applicability of this colorimetric assay can be expanded to other protease biomarkers (e.g., thrombin and hepatitis C virus NS3/4A) by tuning the target-responsive RNA polymerase module. Furthermore, by the immobilization of SNAs on a glass fiber membrane, a test strip that enables the portable detection of target protease with a smartphone was developed. With the use of a mobile application to capture and process the colorimetric signals, this portable detection system allowed for sensitive evaluation of MMP-2 levels in biological and clinical specimens, highlighting its potential in point-of-care diagnosis of diseases.

摘要

生物标志物的灵敏且简便检测对于疾病的早期诊断和治疗至关重要。为此,我们在此提出了一种比色蛋白酶检测法,该方法通过蛋白水解响应转录与球形核酸(SNA)的模块化组合实现。在该检测法中,靶标蛋白酶介导的蛋白水解通过转录触发RNA的合成,随后导致SNA聚集,表面等离子体共振相关吸收波长出现显著红移。作为概念验证,该检测法实现了对基质金属蛋白酶-2(MMP-2)的灵敏且特异性检测,检测限为3.3 pM。此外,通过调整靶标响应RNA聚合酶模块,这种比色检测法的适用性可扩展到其他蛋白酶生物标志物(如凝血酶和丙型肝炎病毒NS3/4A)。此外,通过将SNA固定在玻璃纤维膜上,开发了一种能够用智能手机对靶标蛋白酶进行便携式检测的试纸条。通过使用移动应用程序来捕获和处理比色信号,这种便携式检测系统能够灵敏地评估生物和临床样本中的MMP-2水平,凸显了其在疾病即时诊断中的潜力。

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